Impact Factor
2.26
Journal Citation Impact
Estimated influence, citation density, publishing volume, and citation integrity from the analytics table.
Citation rate
0.98
87 total citations
h5-index
11
h5 depth signal
Cited share
39.8%
37 of 93
Total citations
87
Citation footprint
Metric signal
0.98
External metric anchor
Self-citation
3.4%
3 self-citations
Citations Trend
Monthly Publications Cadence
Citing Geographic Demographics
Japan
267
China
26
Turkey
26
India
21
Pakistan
17
Citing Fields of Research
Congenital Disorders
194
Cytogenetics
138
Genetics & Genomics
91
Cell Differentiation & Development
66
Dentistry & Oral Medicine
59
Publishing Activity & Reach
Volume, recency, access pattern, and citing-community signals from the journal analytics record.
All-time article footprint
1,719
Articles tracked across the journal lifetime
Indexed publication set
93
37 cited publications
Last 12 months
51
25.5 publications/month
Open access share
21.6%
11 OA publications in the last year
Leading citing country
Japan
267 citing publications
Leading citing field
Congenital Disorders
194 citing publications
Latest tracked publication
29 January 2026
10 recent records available
Coverage & Indexing History
v42n1, Mar. 2002-
v42n1, Mar. 2002-
Active Coverage
Research Focus & Classification
Indexed Subjects
Congenital Disorders
Cytogenetics
Dentistry & Oral Medicine
Cell Differentiation & Development
Obstetrics/Gynecology
Issuing & Sponsoring Bodies
Contributor
Nihon Senten Ijō Gakkai
Broad Categories
Teratology
Cytogenetics
Dentistry & Oral Medicine
Cancer & Development
Obstetrics/Gynecology
Abdominal Surgery
MeSH Descriptors
Congenital Abnormalities
Latest Publications
Recent article records with DOI-first linking and condensed abstracts.
01
DOI 10.1002/cga.70043
Open DOI
A C ‐Propeptide Variant in COL1A1 Potentially Perturbing Disulfide Bonding in Osteogenesis Imperfecta Type III
Osteogenesis imperfecta (OI) is a genetic disorder characterized by bone fragility and frequent fractures. The disorder is caused by pathogenic variants in genes that encode type I collagen. The COL1A1 gene encodes the pro‐α1(I) collagen...
02
DOI 10.1002/cga.70042
Open DOI
A Novel MAF Variant Causing Aymé‐Gripp Syndrome With Transient Anemia
03
DOI 10.1002/cga.70039
Open DOI
Worldwide Burden of Urogenital Congenital Anomalies Across Childhood and Adolescence, 1990–2021: Results From the Global Burden of Disease Study 2021
The Burden of urogenital congenital anomalies (UCAs) among children and adolescence aged under 24 years in the world has not been comprehensively studied regarding the Global Burden of Disease Study (GBD) database 2021. This study aims t...
04
DOI 10.1002/cga.70040
Open DOI
Prenatal Diagnosis of Bloom Syndrome Associated With Biallelic BLM RecQ ‐Like Helicase Variants Presenting With Severe Fetal Growth Restriction
Bloom syndrome (BS) is an autosomal recessive disorder characterized by prenatal and postnatal growth deficiency, photosensitive skin changes, immune deficiency, insulin resistance, greatly increased risk of early‐onset cancer, and the d...
05
DOI 10.1002/cga.70036
Open DOI
The Suggestive Association Between the NOG rs227731 Polymorphism and Non‐Syndromic Cleft Lip With or Without Palate Subtypes in a Japanese Cohort
Non‐syndromic cleft lip with or without palate (NSCL/P) ranks among the most prevalent congenital craniofacial anomalies globally. In Japan, reported rates of cleft lip and/or palate range from 1 in 500 to 1 in 700 live births. This stud...
06
DOI 10.1002/cga.70038
Open DOI
How Does the Human Herniated Midgut Loop Return to the Abdominal Cavity?
07
DOI 10.1002/cga.70037
Open DOI
Clinical Outcomes of Twin Reversed Arterial Perfusion ( TRAP ) Sequence: A Retrospective Analysis From a Tertiary Center
Twin Reversed Arterial Perfusion (TRAP) sequence is a rare complication of monochorionic twin pregnancies characterized by reversed blood flow from the pump twin to a nonviable acardiac twin. This study aims to share the clinical outcome...
08
DOI 10.1002/cga.70084
Open DOI
A Clinical and Demographic Investigation on Cases With Multiple Pterygium Syndrome‐Escobar Type
Multiple pterygium syndrome‐Escobar type is a congenital anomaly mostly characterized by the presence of webbing of the skin in major joints but includes a series of other anomalies including vertebral dysmorphisms that need surgical cor...
09
DOI 10.1002/cga.70083
Open DOI
Prenatal Ultrasound and MRI Findings in Two Fetuses With Perineal Lipoma
Congenital perineal lipoma is a rare benign adipose lesion that may present prenatally as a fetal perineal mass. These lesions are frequently associated with ambiguous genitalia, anorectal malformations, and other urogenital anomalies, w...
10
DOI 10.1002/cga.70080
Open DOI
In Ovo Telmisartan Exposure and Developmental Consequences in Embryonic Life Stage of Gallus gallus
Telmisartan, an antihypertensive drug, lowers blood pressure by blocking the angiotensin‐II receptor subtype‐1 (AT1). A few sporadic case studies reported adverse fetal effects of telmisartan in humans. Moreover, there is a scarcity of i...
Bibliographical & Catalog Notes
Quarterly.
Title from cover.
Print issues ceased with 2013.
Also issued online.
Articles chiefly in English; some also in Japanese.
Official journal of the Japanese Teratology Society.
v. 1, no. 1 (JAN 1993)20020918 Notice published Printed on acid-free paper